Actively Recruiting
Detection of Endoscopic Resection Scars and Recurrence Among Non-experts Is Less Accurate Than Experts but Improves with a Short Learning Intervention
Led by University Hospital, Ghent · Updated on 2025-11-25
141
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying how well endoscopists of various experience levels can detect recurrent or residual adenoma (RRA) at the site of an endoscopic mucosal resection scar in colorectal cancer and polyp patients. The study aims to evaluate the accuracy of endoscopic imaging compared to histopathology and to assess the impact of a short video-based learning tool on improving detection skills. This research addresses the risk of missed RRA that could lead to post-colonoscopy colorectal cancer. Participants will first review 15 endoscopic images and answer questions about whether the images show a resection scar, signs of RRA, and their confidence level. They will also indicate how they would treat any detected RRA or suggest alternative diagnoses. After this initial assessment, participants will watch a video-based learning tool focused on detecting RRA. Then, they will evaluate 15 different images using the same questions. All data will be collected online anonymously using pseudonyms. Throughout the study, researchers will analyze responses to measure performance in detecting RRA before and after the learning intervention over a two-year period. They will also compare performance differences among endoscopists with various experience levels. The study uses a secure international image database and involves no direct patient procedures. Participants contribute through an online survey and learning modules, with outcomes focusing on improving non-expert detection of colorectal lesion recurrence.
CONDITIONS
Brief Title
Detection of Endoscopic Resection Scars and Delineation of Recurrence is Trainable
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Endoscopists of any experience level
You will not qualify if you...
- Adults who do not provide consent
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or virtual)
Duration - Up to 2 years
Participants assess endoscopic images prior to and after using a learning tool about detection of endoscopic resection scars and recurrence.
2 assessment sessions (one before and one after the learning tool)
Trial Site Locations
Total: 1 location
1
UZ Gent
Ghent, Belgium, 9000
Actively Recruiting
Research Team
D
David J trate, PhD
S
Sander Smeets, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
2
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